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Amcard (Atenolol)

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Amcard is a beta blocker that works specifically on the heart. It works by slowing down the heart rate and makes the heart more efficient at pumping blood around the body. Amcard is also used to relieve the symptoms caused by an overactive thyroid gland.

Other names for this medication:
Amloact, Amlobet, Amloheart, Amlom, Amlosafe, Amloten, Amlotin, Amlozed, Atcardil, Atekind, Betacard, Cabeta, Camcard, Cemalo, Corvadil, Cyplol, Espil, Exlodep, Gericard, Harten, Latenol, Noldepin, Pdnol, Repalol, Stamlo, Teenol, Tenodipin, Tenoric, Winten

Similar Products:
Effexor, Temovate, Levitra, Dramamine, Aristocort, Caverta, Clozaril, Cipro, Claritin

Also known as: Atenolol


{name} (atenolol) is a beta-blocker that affects the heart and circulation (blood flow through arteries and veins).

{name} is used to treat angina (chest pain) and hypertension (high blood pressure).

{name} is also used to lower the risk of death after a heart attack.


Usual Adult Dose of Amcard for Hypertension:

Initial dose: 50 mg orally once a day Maintenance dose: 50 to 100 mg orally once a day Maximum dose: 100 mg per day Comments: -If desired response not achieved after 1 to 2 weeks, increase to 100 mg may be beneficial. -Doses greater than 100 mg once a day did not result in significant additional antihypertensive effects. Use: For the treatment of hypertension alone or in combination with other antihypertensive agents.

Usual Adult Dose of Amcard for Angina Pectoris Prophylaxis:

Initial dose: 50 mg orally once a day -Increase to 100 mg orally once a day after 1 week if optimal response not achieved Maintenance dose: 50 to 200 mg orally once a day Maximum dose: 200 mg per day Comments: -Some patients may require 200 mg per day to attain optimal effect. Use: For the long-term management of angina pectoris due to coronary atherosclerosis.

Usual Adult Dose for Angina Pectoris:

Initial dose: 50 mg orally once a day -Increase to 100 mg orally once a day after 1 week if optimal response not achieved Maintenance dose: 50 to 200 mg orally once a day Maximum dose: 200 mg per day Comments: -Some patients may require 200 mg per day to attain optimal effect. Use: For the long-term management of angina pectoris due to coronary atherosclerosis.

Usual Adult Dose of Amcard for Myocardial Infarction:

50 mg orally twice a day or 100 mg orally once a day Comments: -If IV beta blockers are contraindicated or inappropriate, oral therapy should continue for at least 7 days post-myocardial infarction (MI). -Treatment with beta blockers post MI should generally continue for 1 to 3 years if there are no contraindications. Use: For the management of hemodynamically stable patients with definite or suspected acute myocardial infarction to reduce cardiovascular mortality.

Usual Geriatric Dose for Hypertension:

Initial dose: Consider reducing the starting dose to 25 mg orally once a day

Detailed Amcard dosage information


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include extreme weakness or lack of energy, very slow heart rate, shortness of breath, or fainting.


Store at room temperature between 20 and 25 degrees C (68 and 77 degrees F) away from moisture and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Amcard are:

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Hepatic capsular retraction secondary to involuting cavernous hemangioma. The information gathered from this work confirms the primary role of water molecules and protein flexibility in docking-based studies and can be exploited to aid NS5B-directed HCV drug discovery efforts. ANIT-intoxicated rats received alpha-Toc (100 or 250 mg/kg) or melatonin (100 mg/kg) orally at 12 h after intoxication. The cumulative probability of Nd:YAG laser posterior capsulotomy was calculated by Kaplan-Meier estimates, and risk factors were analyzed using the Cox proportional hazards model. Body temperature was recorded by nasal cannula and compared with the baseline temperature at the neurovascular bundle. From each participant, four digital photographs of the superior and inferior conjunctivae of both eyes, with a fixed succession of photography (right upper, right lower, left upper, left lower), were taken with a slit lamp mounted camera. A good practice protocol is proposed at the end of the manuscript. We show that with an in-plane external magnetic field an anomalous supercurrent appears even for zero phase difference between the superconducting electrodes. When preprocessing time is factored in, the run time ratio PMS5/PMS6 is as high as 2.75 for (13,4) instances and as low as 1.95 for (17,6) instances.

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Recent morphometric studies by magnetic resonance imaging have produced conflicting results regarding the extent of grey and white matter involvement in ALS patients. Our data clearly identify important anti-inflammatory properties of the minor surfactant phospholipids at the environmental interface of the lung. In newborns, vasopressin binding sites of the V1a type were present in all laminae of the central gray at all segmental levels, whereas oxytocin binding sites were found only in the superficial layers of the dorsal horn. Therefore, the functional impact of glutathionylated actin on the interaction with myosin-S1 was examined. Mechanism of toxic action of methyl methacrylate used in prosthodontics. The pharmacokinetics of levosalbutamol: what are the clinical implications?. Our data show that haploinsufficiency of Tbx1 is sufficient to generate at least one important component of the DiGeorge syndrome phenotype in mice, and demonstrate the suitability of the mouse for the genetic dissection of microdeletion syndromes. Upon exposure to cadmium (4.25 micromol L(-1) and 8.5 micromol L(-1)) for 48 h, the mRNA expression of LvABCG was up-regulated 4.79-fold (at 6 h) and 2.09-fold (at 12 h) in the hepatopancreas. Case report: A rare cause of miliary nodules -- allergic bronchopulmonary aspergillosis. The labeled proteins were microinjected intravitreally into the normal or light damaged rat eye and each eye collected at three intervals after the injections.

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